Optical Analysis Systems and Methods for Dynamic, High-Speed Detection and Real-Time Multivariate Optical Computing

ABSTRACT

Multivariate optical analysis systems employ multivariate optical elements and utilize multivariate optical computing methods to determine information about a product carried by light reflected from or transmitted through the product. One method of processing and monitoring the product includes introducing the product at an inspection point; illuminating the product with a spectral-specific light though an optic lens; directing the light that has passed through at least a section of the product through at least one multivariate optical element to produce a first signal, the directed light carrying information about the product; detecting the first signal at a first detector; deflecting a portion of the directed light to produce a second signal in a direction of a second detector, the second detector configured to detect the second signal; and determining at least one property of the product at a rate of about one section of the product per second to about five sections of the product per second based upon the detector outputs.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims benefit of U.S. Provisional Patent Application, Ser. No. 60/781,007, and U.S. Provisional Patent Application, Ser. No. 60/781,028, both filed Mar. 10, 2006, and both incorporated herein by reference thereto in their entireties.

BACKGROUND OF THE DISCLOSURE

Light conveys information through data. When light interacts with matter, for example, it carries away information about the physical and chemical properties of the matter. A property of the light, such as its intensity, may be measured and interpreted to provide information about the matter with which the light interacted. That is, the data carried by the light through its intensity may be measured to derive information about the matter. Similarly, in optical communications systems, light data is manipulated to convey information over an optical transmission medium, for example, fiber optic cable. The data is measured when the light signal is received to derive information.

In general, a simple measurement of light intensity is difficult to convert to information because it likely contains interfering data. That is, several factors may contribute to the intensity of light, even in a relatively restricted wavelength range. It is often impossible to adequately measure the data relating to one of these factors since the contribution of the other factors is unknown.

It is possible, however, to derive information from light. An estimate may be obtained, for example, by separating light from several samples into wavelength bands and performing a multiple linear regression of the intensity of these bands against the results of conventional measurements of the desired information for each sample. For example, a polymer sample may be illuminated so that light from the polymer carries information such as the sample's ethylene content. Light from each of several samples may be directed to a series of bandpass filters which separate predetermined wavelength bands from the light. Light detectors following the bandpass filters measure the intensity of each light band. If the ethylene content of each polymer sample is measured using conventional means, a multiple linear regression of ten measured bandpass intensities against the measured ethylene content for each sample may produce an equation such as:

y=a ₀ +a ₁ w ₁ +a ₂ w ₂ + . . . +a ₁₀ w ₁₀   (“Equation 1”)

where y is ethylene content, a_(n) are constants determined by the regression analysis, and w_(n) is light intensity for each wavelength band.

Equation 1 may be used to estimate ethylene content of subsequent samples of the same polymer type. Depending on the circumstances, however, the estimate may be unacceptably inaccurate since factors other than ethylene may affect the intensity of the wavelength bands. These other factors may not change from one sample to the next in a manner consistent with ethylene.

A more accurate estimate may be obtained by compressing the data carried by the light into principal components. To obtain the principal components, spectroscopic data is collected for a variety of samples of the same type of light, for example from illuminated samples of the same type of polymer. For example, the light samples may be spread into their wavelength spectra by a spectrograph so that the magnitude of each light sample at each wavelength may be measured. This data is then pooled and subjected to a linear-algebraic process known as singular value decomposition (SVD). SVD is at the heart of principal component analysis, which should be well understood in this art. Briefly, principal component analysis is a dimension reduction technique, which takes m spectra with n independent variables and constructs a new set of eigenvectors that are linear combinations of the original variables. The eigenvectors may be considered a new set of plotting axes. The primary axis, termed the first principal component, is the vector, which describes most of the data variability. Subsequent principal components describe successively less sample variability, until only noise is described by the higher order principal components.

Typically, the principal components are determined as normalized vectors. Thus, each component of a light sample may be expressed as x_(n) z_(n), where x_(n) is a scalar multiplier and z_(n) is the normalized component vector for the n_(th) component. That is, z_(n) is a vector in a multi-dimensional space where each wavelength is a dimension. As should be well understood, normalization determines values for a component at each wavelength so that the component maintains it shape and so that the length of the principal component vector is equal to one. Thus, each normalized component vector has a shape and a magnitude so that the components may be used as the basic building blocks of all light samples having those principal components. Accordingly, each light sample may be described in the following format by the combination of the normalized principal components multiplied by the appropriate scalar multipliers:

x₁z₁+x₂z₂+ . . . +x_(n)z_(n).

The scalar multipliers x_(n) may be considered the “magnitudes” of the principal components in a given light sample when the principal components are understood to have a standardized magnitude as provided by normalization.

Because the principal components are orthogonal, they may be used in a relatively straightforward mathematical procedure to decompose a light sample into the component magnitudes, which accurately describe the data in the original sample. Since the original light sample may also be considered a vector in the multi-dimensional wavelength space, the dot product of the original signal vector with a principal component vector is the magnitude of the original signal in the direction of the normalized component vector. That is, it is the magnitude of the normalized principal component present in the original signal. This is analogous to breaking a vector in a three dimensional Cartesian space into its X, Y and Z components. The dot product of the three-dimensional vector with each axis vector, assuming each axis vector has a magnitude of 1, gives the magnitude of the three dimensional vector in each of the three directions. The dot product of the original signal and some other vector that is not perpendicular to the other three dimensions provides redundant data, since this magnitude is already contributed by two or more of the orthogonal axes.

Because the principal components are orthogonal, or perpendicular, to each other, the dot, or direct, product of any principal component with any other principal component is zero. Physically, this means that the components do not interfere with each other. If data is altered to change the magnitude of one component in the original light signal, the other components remain unchanged. In the analogous Cartesian example, reduction of the X component of the three dimensional vector does not affect the magnitudes of the Y and Z components.

Principal component analysis provides the fewest orthogonal components that can accurately describe the data carried by the light samples. Thus, in a mathematical sense, the principal components are components of the original light that do not interfere with each other and that represent the most compact description of the entire data carried by the light. Physically, each principal component is a light signal that forms a part of the original light signal. Each has a shape over some wavelength range within the original wavelength range. Summing the principal components produces the original signal, provided each component has the proper magnitude.

The principal components comprise a compression of the data carried by the total light signal. In a physical sense, the shape and wavelength range of the principal components describe what data is in the total light signal while the magnitude of each component describes how much of that data is there. If several light samples contain the same types of data, but in differing amounts, then a single set of principal components may be used to exactly describe (except for noise) each light sample by applying appropriate magnitudes to the components.

The principal components may be used to accurately estimate information carried by the light. For example, suppose samples of a certain brand of gasoline, when illuminated, produce light having the same principal components. Spreading each light sample with a spectrograph may produce wavelength spectra having shapes that vary from one gasoline sample to another. The differences may be due to any of several factors, for example differences in octane rating or lead content.

The differences in the sample spectra may be described as differences in the magnitudes of the principal components. For example, the gasoline samples might have four principal components. The magnitudes x_(n) of these components in one sample might be J, K, L, and M, whereas in the next sample the magnitudes may be 0.94 J, 1.07K, 1.13 L and 0.86M. As noted above, once the principal components are determined, these magnitudes exactly describe their respective light samples.

Refineries desiring to periodically measure octane rating in their product may derive the octane information from the component magnitudes. Octane rating may be dependent upon data in more than one of the components. Octane rating may also be determined through conventional chemical analysis. Thus, if the component magnitudes and octane rating for each of several gasoline samples are measured, a multiple linear regression analysis may be performed for the component magnitudes against octane rating to provide an equation such as:

y=a ₀ +a ₁ x ₁ +a ₂ x ₂ +a ₃ x ₃ +a ₄ x4  (“Equation 2”)

where y is octane rating, an are constants determined by the regression analysis, and x₁, x₂, x₃ and x₄ are the first, second, third and fourth principal component magnitudes, respectively.

Using Equation 2, which may be referred to as a regression vector, refineries may accurately estimate octane rating of subsequent gasoline samples. Conventional systems perform regression vector calculations by computer, based on spectrograph measurements of the light sample by wavelength. The spectrograph system spreads the light sample into its spectrum and measures the intensity of the light at each wavelength over the spectrum wavelength range. If the regression vector in the Equation 2 form is used, the computer reads the intensity data and decomposes the light sample into the principal component magnitudes x_(n) by determining the dot product of the total signal with each component. The component magnitudes are then applied to the regression equation to determine octane rating.

To simplify the procedure, however, the regression vector is typically converted to a form that is a function of wavelength so that only one dot product is performed. Each normalized principal component vector z_(n) has a value over all or part of the total wavelength range. If each wavelength value of each component vector is multiplied by the regression constant a_(n) corresponding to the component vector, and if the resulting weighted principal components are summed by wavelength, the regression vector takes the following form:

y=a ₀ +b ₁ u ₁ +b ₂ u ₂ + . . . +b _(n) u _(n)  (“Equation 3”)

where y is octane rating, a₀ is the first regression constant from Equation 2, b_(n) is the sum of the multiple of each regression constant a_(n) from Equation 2 and the value of its respective normalized regression vector at wavelength n, and u_(n) is the intensity of the light sample at wavelength n. Thus, the new constants define a vector in wavelength space that directly describes octane rating. The regression vector in a form as in Equation 3 represents the dot product of a light sample with this vector.

Normalization of the principal components provides the components with an arbitrary value for use during the regression analysis. Accordingly, it is very unlikely that the dot product result produced by the regression vector will be equal to the actual octane rating. The number will, however, be proportional to the octane rating. The proportionality factor may be determined by measuring octane rating of one or more samples by conventional means and comparing the result to the number produced by the regression vector. Thereafter, the computer can simply scale the dot product of the regression vector and spectrum to produce a number approximately equal to the octane rating.

In a conventional spectroscopy analysis system, a laser directs light to a sample by a bandpass filter, a beam splitter, a lens and a fiber optic cable. Light is reflected back through the cable and the beam splitter to another lens to a spectrograph. The spectrograph separates light from the illuminated sample by wavelength so that a detection device such as a charge couple detector can measure the intensity of the light at each wavelength. The charge couple detector is controlled by controller and cooled by a cooler. The detection device measures the light intensity of light from the spectrograph at each wavelength and outputs this data digitally to a computer, which stores the light intensity over the wavelength range. The computer also stores a previously derived regression vector for the desired sample property, for example octane, and sums the multiple of the light intensity and the regression vector intensity at each wavelength over the sampled wavelength range, thereby obtaining the dot product of the light from the substance and the regression vector. Since this number is proportional to octane rating, the octane rating of the sample is identified.

Since the spectrograph separates the sample light into its wavelengths, a detector is needed that can detect and distinguish the relatively small amounts of light at each wavelength. Charge couple devices provide high sensitivity throughout the visible spectral region and into the near infrared with extremely low noise. These devices also provide high quantum efficiency, long lifetime, imaging capability and solid-state characteristics. Unfortunately, however, charge couple devices and their required operational instrumentation are very expensive. Furthermore, the devices are sensitive to environmental conditions. In a refinery, for example, they must be protected from explosion, vibration and temperature fluctuations and are often placed in protective housings approximately the size of a refrigerator. The power requirements, cooling requirements, cost, complexity and maintenance requirements of these systems have made them impractical in many applications.

Multivariate optical computing (MOC) is a powerful predictive spectroscopic technique that incorporates a multi-wavelength spectral weighting directly into analytical instrumentation. This is in contrast to traditional data collection routines where digitized spectral data is post processed with a computer to correlate spectral signal with analyte concentration. Previous work has focused on performing such spectral weightings by employing interference filters called Multivariate Optical Elements (MOEs). Other researchers have realized comparable results by controlling the staring or integration time for each wavelength during the data collection process. All-optical computing methods have been shown to produce similar multivariate calibration models, but the measurement precision via an optical computation is superior to a traditional digital regression.

MOC has been demonstrated to simplify the instrumentation and data analysis requirements of a traditional multivariate calibration. Specifically, the MOE utilizes a thin film interference filter to sense the magnitude of a spectral pattern. A no-moving parts spectrometer highly selective to a particular analyte may be constructed by designing simple calculations based on the filter transmission and reflection spectra. Other research groups have also performed optical computations through the use of weighted integration intervals and acousto-optical tunable filters digital mirror arrays and holographic gratings.

The measurement precision of digital regression has been compared to various optical computing techniques including MOEs, positive/negative interference filters and weighted-integration scanning optical computing. In a high signal condition where the noise of the instrument is limited by photon counting, optical computing offers a higher measurement precision when compared to its digital regression counterpart. The enhancement in measurement precision for scanning instruments is related to the fraction of the total experiment time spent on the most important wavelengths. While the detector integrates or coadds measurements at these important wavelengths, the signal increases linearly while the noise increases as a square root of the signal. Another contribution to this measurement precision enhancement is a combination of the Felgott's and Jacquinot's advantage, which is possessed by MOE optical computing.

SUMMARY OF THE DISCLOSURE

The present disclosure is directed generally to optical analysis systems using real-time multivariate optical computing. Multivariate optical computing (MOC) is a predictive spectroscopy technique that incorporates a multi-wavelength spectral weighting directly into analytical instrumentation. MOC is generally described in U.S. Pat. No. 6,198,531 B1 to Myrick et al. and in U.S. Pat. No. 6,529,276 B1 to Myrick, both of which are incorporated herein for all purposes by reference thereto.

Since multivariate optical element (MOE)-based MOC uses detectors that see all wavelengths emanating from an illumination source simultaneously—including wavelengths that carry no information—measurement noise is reduced and measurement precision is increased in a system of the present disclosure by making the system sensitive primarily to wavelengths carrying information. Additionally, the exemplary system controls a spectral range of the illumination source by using bandpass filters or spectral elements having predetermined transmission characteristics. Further, in some aspects of the present disclosure, the system shines a light signal directly onto a sample and eliminates the use of, for instance, a fiber optic probe; therefore, the component parts of the disclosure are simple and economical to manufacture, assemble and use, with improved signals when the attenuation typical of a fiber optic probe is removed. These and other aspects and advantages of the present disclosure will be apparent from the following description and the attached drawings, or can be learned through practice of the exemplary systems and methods according to the disclosure.

According to a particular embodiment of the present disclosure, an optical analysis system generally includes an illumination source for shining light or other radiative energy through a set of lenses. Light levels are maximized through the optical system to enhance transmission (reduce loss) of the light. The illumination source subsequently shines the light through a multi-window (e.g., 10-window) chopper wheel. The chopper wheel rotates, for instance, at 40 Hertz (Hz), which produces a light beam modulated at 400 Hz. A modulated light signal is beneficial for reliable performance of the photodetectors in the system.

Further in this aspect, the light beam may pass through one or more spectral elements or filters, which control the spectral region of the light that passes through the elements or filters (and onto a sample). The light may be reflected by a turning mirror down the center of the sampling tube and focused by a lens on the sample. The light is reflected back by the sample through the lens and back down the sampling tube, past the turning mirror. The light may pass through a beam splitter which reflects part of the light (“signal A”) through an MOE and lens and onto a photodetector. Another part of the light (“signal B”) may pass through a lens onto another photodetector and act as a reference signal. Thus, the system may measure signal A and signal B, and a ratio of the two signals may be used to measure a concentration of the sample, e.g., a chemical of interest. Additionally, monitoring of signal A and/or signal B independently, or in some combination, can provide other information, such as powder segregation, packing of materials, effect of particle size. More specifically, any algebraic combination of signals A and B can be used according to the disclosure; e.g., A and/or B independently; A divided by B; A plus B; A minus B; B divided by A; B minus A, etcetera. For example, a ratio of signal A to signal B can provide a chemical measurement; individually, A signal and/or B signal can provide other homogeneity measures including physical make-up of the sample, packing, particle size, and/or separate physical and chemical properties.

According to another aspect of the disclosure, a method of determining information carried by light may include providing an optical analysis system having a multivariate optical element disposed to receive a source light from an illumination source; filtering the source light through a spectral element in the optical element analysis system; reflecting the filtered light through an inner region of a cavity in a first direction of a sample to be measured, the cavity defining a second region disposed about the inner region; focusing the reflected light proximate the sample; reflecting the focused light from the sample through the second region in a second direction of a beamsplitter, the light being reflected from the sample carrying data from the sample; splitting the sample carrying light with the beamsplitter into a first light and a second light; optically filtering the data of the first light with the multivariate optical element into an orthogonal component; directing the first light filtered by the multivariate optical element onto a first photodetector; directing the second light onto a second photodetector; and comparing the orthogonal component to information present in the second light to determine a property of the sample. Also in this aspect, the light may be focused on, in or near the sample, the light having a focal point proximate the sample. Also in this aspect, the beamsplitter may be a 50/50 beamsplitter.

The method in this aspect may also include modulating the light from about 50 Hz to about 5000 Hz before filtering the light through the spectral element. Further, the method may include controlling a spectral range of the light source, and the spectral element may have a predetermined transmission characteristic for controlling the spectral range. Also in this aspect, the spectral element may be two or more spectral elements for controlling the spectral range of the light source.

The method may further include measuring a concentration of the sample ratio using a ratio of the first light and the second light. Additionally, the method may include monitoring the first light, the second light or combinations thereof to assess particle segregation of the sample; monitoring the first light, the second light or combinations thereof to assess density of the sample; monitoring the first light, the second light or combinations thereof to assess affect of particle size in the sample; monitoring the first light, the second light or combinations thereof to measure a chemical in the sample; monitoring the first light, the second light or combinations thereof to measure homogeneity of the sample and combinations of the foregoing steps.

Also in this aspect of the disclosure, the method may include using a fiber optic probe. Moreover, the method may include preparing a chemometric model to make a similar measurement of the light reflected from the sample as a measurement made by the optical analysis system. The method may also use the illumination light from the outer annular region with the filtered light through the inner region of the cavity to determine the property of the sample.

In yet another aspect of the disclosure, an optical analysis system may be configured in a transmission mode rather than a reflectance mode as in the foregoing embodiments. In the transmission mode, light would pass through a sample (e.g., a fluid sample) and be collected on a far side of the sample to enable, for instance, study of particle density in the fluid sample in conjunction with a chemical content. More particularly, the optical analysis system in this aspect may be configured to operate in the transmission mode in which the light is shone through the sample to a similar detection system. Additionally, or alternatively, a mirrored surface may be placed within the transmissive sample to reflect the light back into the detection system as described above.

In another aspect of the disclosure, a method of determining information carried by light may include determining a plurality of orthogonal components of a first portion of a light signal, wherein each of the components has a predetermined shape with respect to a property of the first portion of the light signal that varies over a predetermined wavelength range; determining respective weightings for the orthogonal components so that the magnitude of the orthogonal components in the first portion of the light signal, weighted by the weightings, is proportional to the information present in the first portion in a predetermined relationship; providing an optical filter mechanism configured to optically filter the orthogonal components; disposing the optical filter mechanism to receive the first portion of the light signal; disposing a detector to receive a second portion of the light signal; detecting the property of the first portion of the light signal filtered by the optical filter mechanism; and analyzing the sample in real time by comparing the property of the first portion of the light signal to information in the second portion of the light signal.

In yet another aspect of the disclosure, an optical analysis system may include a light source being configured to radiate a first light along a first ray path; a modulator disposed in the first ray path, the modulator being configured to modulate the first light to a desired frequency; a spectral element disposed proximate the modulator, the spectral element being configured to filter the first light for a spectral range of interest of a liquid sample; a cavity in communication with the spectral element, the cavity being configured to direct the first light in a direction of the liquid sample; a retroreflector such as a mirror being configured to convert the first light reflecting from the liquid sample into a second light, the cavity being further configured to direct the second light; a beamsplitter being configured to split the second light into a first beam and a second beam; an optical filter mechanism disposed to receive the first beam, the optical filter mechanism being configured to optically filter data carried by the first beam into at least one orthogonal component of the first beam; a first detector mechanism in communication with the optical filter mechanism to measure a property of the orthogonal component to measure the data; and a second detector mechanism being configured to receive the second beam for comparison of the property of the orthogonal component to the second beam. The mirror, such as a conical or flat mirror, in this aspect may include a coating of gold, aluminum or other element or material selected based on desired spectral region.

In another aspect of the disclosure, a method of high-speed processing and monitoring may include moving a product past an inspection point; illuminating at least a portion of the product with a light; directing light carrying information about the portion through at least one multivariate optical element to produce a first signal; detecting the first signal at a first detector; detecting a deflected portion of the light at a second detector; and determining at high speed at least one selected property of the portion as the portion moves past the inspection point based upon the detector outputs. The product in this aspect may be a pharmaceutical tablet, a pharmaceutical powder, a liquid, a gas, an emulsion, a solution, and a mixture.

In another aspect of the disclosure, a method of real-time processing and monitoring may include blending a material of interest with a secondary material; illuminating the blended materials with a light; reflecting light carrying information about the blended materials through at least one multivariate optical element to produce a first signal; detecting the first signal at a first detector detecting a deflected portion of the light at a second detector; and determining, in real time, at least one selected property of at least one of the blended materials as the material of interest and the secondary material are blended based upon respective detector outputs. In this aspect, real time may be defined as being faster than about 30 seconds, preferably faster than about 5 seconds, more preferably faster than about 1 second, still more preferably faster than about 1/10 of a second, yet more preferably faster than about 1/100 of a second, and most preferably faster than about 1/1000 of a second.

In a further aspect of the disclosure, a method of real-time pharmaceutical processing and monitoring may include blending a pharmaceutical powder by mixing an active agent with an excipient; illuminating the pharmaceutical powder with a spectral-specific light though an optic window, the optic window configured to focus the spectral-specific light into the pharmaceutical powder; reflecting light carrying information about the pharmaceutical powder through at least one multivariate optical element to produce a first signal; detecting the first signal at a first detector; detecting a deflected portion of the spectral-specific light at a second detector; and determining, in real time, at least one selected property of the pharmaceutical powder as the pharmaceutical powder is blended based upon respective detector outputs. In this aspect, the selected property of the pharmaceutical powder may be an active property of the active agent. Also in this aspect, the selected property may be a particulate size of the active agent. The selected property may also be a secondary property of the excipient. Furthermore, in this aspect of the disclosure a homogeneity asymptote of the pharmaceutical powder can be assessed.

In yet another aspect of the disclosure, a method of real-time pharmaceutical processing and monitoring is provided wherein real time may be defined as being between about 1/1000 of a second to about 30 seconds. The method may include illuminating a fluid in a container with a spectral-specific light though an optic window disposed proximate an aperture in a conduit in communication with the container; reflecting light carrying information about the fluid through at least one multivariate optical element to produce a first signal; detecting the first signal at a first detector; deflecting a portion of the spectral-specific light with a retroreflecting mirror; detecting the deflected portion at a second detector; and determining, in real time, at least one selected property of the fluid as the fluid flows past the optic window based on the detector outputs. The fluid in this aspect may be opaque in appearance. Moreover, the fluid may be a liquid chemical and the window may be configured to focus the spectral-specific light into the liquid chemical. The liquid chemical may also be a blend of at least one active pharmaceutical agent and at least one excipient. Alternatively, the fluid may be a gas, which may be clear or opaque.

In another aspect of the disclosure, a method of real-time processing and monitoring may include mixing a material of interest with a secondary material; illuminating the materials with a light; reflecting light carrying information about the materials through at least one multivariate optical element to produce a first signal; detecting the first signal at a first detector; detecting a deflected portion of the light at a second detector; and determining, in real time, at least one selected property of at least one of the materials based upon respective detector outputs. The selected property in this aspect may be determined based upon a compositional change. The compositional change may include a chemical reaction. Further, the compositional change may include a crystallization process.

In another aspect of the disclosure, a method of high-speed pharmaceutical processing and monitoring may include moving a plurality of portions of pharmaceutical product past an inspection point; illuminating at least one portion of the pharmaceutical product with a spectral-specific light though an optic window, the window configured to focus the spectral-specific light onto a portion at the inspection point; reflecting light carrying information about the portion through at least one multivariate optical element to produce a first signal; detecting the first signal at a first detector; detecting a deflected portion of the spectral-specific light at a second detector; and determining at high speed at least one selected property of the portion as the portion moves past the inspection point based upon the detector outputs. In this aspect, the portion may be a pharmaceutical tablet or a quantity of pharmaceutical powder. The portion may be a chemical sample in a closed container, and the container may be at least partially transparent to light focused onto the chemical sample.

According to this aspect of the disclosure, the portion may be moved past the inspection point in at least one minute, preferably in at least 10 seconds. Still more preferably, at least 10 portions per second may be moved past the inspection point.

In a further aspect of the disclosure, a method of processing and monitoring a solid phase may include moving a solid product past an inspection point; illuminating the solid product with a spectral-specific light though an optic lens; reflecting light from the solid product through at least one multivariate optical element to produce a first signal, the reflected light carrying information about the solid product; detecting the first signal at a first detector; deflecting a portion of the reflected light in a direction of a second detector, the second detector configured to detect the deflected portion; and computing at high speed at least one selected property of the solid product as the solid product moves past the inspection point based upon the detector outputs. In this aspect, the solid product may be a pharmaceutical tablet or a quantity of pharmaceutical powder. Also in this aspect of the disclosure, the solid product may be a powder mixture in a closed container, and the container may be at least partially transparent to light focused onto the powder mixture.

In another aspect of the disclosure, an optical analysis system may include a light source being configured to radiate a first light along a first ray path; a modulator disposed in the first ray path, the modulator being configured to modulate the first light to a desired frequency; a spectral element disposed proximate the modulator, the spectral element being configured to filter the first light for a spectral range of interest of a sample, e.g., a liquid, the first light being directed into the sample; a conical mirror being configured to convert the first light from the sample into a second light; a beamsplitter being configured to split the second light into a first beam and a second beam; an optical filter mechanism disposed to receive the first beam, the optical filter mechanism being configured to optically filter data carried by the first beam into at least one orthogonal component of the first beam; a first detector mechanism in communication with the optical filter mechanism to measure a property of the orthogonal component to measure the data; and a second detector mechanism being configured to receive the second beam for comparison of the property of the orthogonal component to the second beam. The conical mirror may include a coating of gold or aluminum, and may be a collimating mirror configured to diffuse the first light into the second light.

In this aspect of the disclosure, the optical analysis system may further include a cavity in communication with the spectral element, the cavity being configured to direct the first light in a direction of the sample. The cavity may be specular and configured to direct the second light to avoid attenuation.

According to yet another aspect of the disclosure, an optical analysis system may include a light source being configured to radiate a first light along a first ray path; a modulator disposed in the first ray path, the modulator being configured to modulate the first light to a desired frequency; a spectral element disposed proximate the modulator, the spectral element being configured to filter the first light for a spectral range of interest of a sample; a light diversion path for diverting the first light into the sample, the first light being transmitted through the sample and emerging as a second light; a beamsplitter being configured to split the second light into a first beam and a second beam; an optical filter mechanism disposed to receive the first beam, the optical filter mechanism being configured to optically filter data carried by the first beam into at least one orthogonal component of the first beam; a first detector mechanism in communication with the optical filter mechanism to measure a property of the orthogonal component to measure the data; and a second detector mechanism being configured to receive the second beam for comparison of the property of the orthogonal component to the second beam. The light diversion path, for example, may be a fiber-optic cable or a plurality of mirrors arranging a linear or tortuous light path.

In another aspect of the disclosure, a method of high-speed processing and monitoring may include moving a product past an inspection point; illuminating at least a section of the product with a light; directing the light that has passed through the section and is carrying information about the product through at least one multivariate optical element to produce a first signal; deflecting a portion of the light to produce a second signal; detecting the first signal at a first detector; detecting the second signal at a second detector; and determining at least one property of the product based upon the detector outputs as the product moves past the inspection point at a rate of about one section per second to about five sections per second. The product may be a solid product, a liquid product or a gas product. The solid product may be a pharmaceutical tablet or a pharmaceutical powder. Moreover, the product may be an emulsion, a solution, or a mixture.

Also in this aspect, an illumination source for the light may be disposed or positioned proximate the section of the product and the light that has passed through the section may be reflected from the section in a direction of the detectors. Alternatively, or additionally, the illumination source may be disposed proximate the product and the light that has passed through the section may transmit through the product in a direction of the detectors.

The method may further include diverting a part of the light from the illumination source into the product along a light diversion path. The light diversion path may be a fiber-optic cable or a series of mirrors. The method may also include diffusing the light that has passed through the section before the light is directed to the multivariate optical element. The light may be diffused by a collimating mirror.

In an additional aspect of the disclosure, a method of processing and monitoring a product may include introducing a product at an inspection point; illuminating the product with a spectral-specific light though an optic lens; directing the light that has passed through at least a section of the product through at least one multivariate optical element to produce a first signal, the directed light carrying information about the product; detecting the first signal at a first detector; deflecting a portion of the directed light to produce a second signal in a direction of a second detector, the second detector configured to detect the second signal; and determining at least one property of the product at a rate of about one section of the product per second to about five sections of the product per second based upon the detector outputs. The product may be a solid, liquid or gas and be disposed in a closed container. The container may be at least partially transparent to light focused onto the product. The product may be moved past the inspection point and/or the optic lens may be moved past the product.

BRIEF DESCRIPTION OF THE DRAWINGS

A full and enabling disclosure of the present exemplary systems and methods, including the best mode thereof to one skilled in the art, is set forth more particularly in the remainder of the specification, including reference to the accompanying figures, in which:

FIG. 1 is a top perspective view of one embodiment of a real time measurement system according to an aspect of the present disclosure;

FIG. 2 is a schematic view of a concentric cavity as in FIG. 1 in accordance with a further aspect of the present disclosure;

FIG. 3 is schematic plan view of another embodiment of a real time measurement system particularly showing a retroreflecting mirror for use with clear materials according to another aspect of the present disclosure;

FIG. 4A is a perspective view of the retroreflecting mirror as in FIG. 3;

FIG. 4B is an end view of the retroreflecting mirror as in FIG. 4A;

FIG. 5 is a cross section of the retroreflecting mirror taken along line V-V in FIG. 4B;

FIG. 6 is a cross section of a conventional mirror;

FIG. 7 is a schematic view of an implementation in which a material may be measured in real-time;

FIG. 8 is another schematic view of a real-time process measurement using the present disclosure;

FIG. 9 is a schematic view of multiple process stages for monitoring material characteristics according to the disclosure;

FIG. 10 is a schematic plan view of another embodiment of a real time measurement system according to another aspect of the disclosure; and

FIG. 11 is a schematic view of an exemplary measurement process according to a further aspect of the disclosure.

DETAILED DESCRIPTION OF THE DISCLOSURE

Detailed reference will now be made to the drawings in which examples embodying aspects of the present disclosure are shown. The detailed description uses numerical and letter designations to refer to features of the drawings. Like or similar designations of the drawings and description have been used to refer to like or similar parts of the disclosure.

The drawings and detailed description provide a full and written description of the disclosure, and of the manner and process of making and using it, so as to enable one skilled in the pertinent art to make and use it, as well as the best mode of carrying out the disclosure. However, the examples set forth in the drawings and detailed description are provided by way of explanation only and are not meant as limitations of the disclosure. The present disclosure thus includes any modifications and variations of the following examples as come within the scope of the appended claims and their equivalents.

As used herein, the term “light” is broadly used to mean any form of radiation or radiative energy including, for instance, visible light or light in the infrared region. “Light” is also referred to herein as a light signal, a light beam, a light ray and the like to mean any form of radiative energy in the electromagnetic spectrum. Similarly, the term “transmission” can mean transmission of radiative energy onto a surface of a sample; penetration, however slight, into a sample such as a particulate sample or opaque fluid sample; or passage through a sample such as a fluid sample.

As used herein, a sample W (alternatively, workpiece or material M) can mean an analyte undergoing analysis over a range of conditions. The sample W can be a solid or a fluid including but not limited to a powder, a pharmaceutical powder mixed with lactose and other excipient materials, a chemical, a polymer, a petroleum product, a solution, a dispersion, an emulsion and combinations of these solids and fluids.

As generally shown in FIGS. 1 and 2, an optical analysis system according to an aspect of the disclosure is designated by the element number 10. The system 10 is designed around at least one application specific multivariate optical element (MOE) based on spectra typically provided by an end-user. The system design takes into account representative spectra of compounds of interest, basic and expected concentrations of interest across a range of expected interferents. Also, the system 10 incorporates the desired spectral regions (UV, VIS, NIR, MIR, IR) of interest.

In the embodiment shown in FIG. 1, the optical analysis system 10 broadly includes a housing 12, a plurality of illumination or light sources 14A, 14B, a concentric light tube or cavity 22, a focusing lens 26, at least one beam splitter 28, a first detector 30 including a multivariate optical element 48 and a second detector 32. Although FIG. 1 shows a generally square or rectangle shaped, metallic housing 12 and two detectors 30, 32 arranged therein, the skilled artisan will instantly appreciate that a variety of shapes, dimensions, component placements and material makeup of the components can be substituted for the examples shown according to various requirements such as government regulations, customer specifications and the like. Moreover, as discussed below with respect to an embodiment of the disclosure, the sample W can be analyzed using a PCR-type model without a/or beamsplitter 28 in an off-line approach.

The skilled artisan will also understand that although the system 10 can be a measurement system operating in reflectance mode, the system 10 can also be configured to operate in a transmission mode in which light is shone through the sample W from an incident side of the sample W to a similar detection system 110 on another side of the sample W. Alternatively, or additionally, a mirrored surface 210 can be placed within the transmissive sample W to reflect the light back into the detection system 10. Therefore, the disclosure is not limited only to the examples shown in the figures.

With more particular reference to FIG. 1, the housing 12 (shown partially in phantom for clarity) can be metal such as stainless steel, a plastic material such as high-density polyethylene (HDPE) or any durable material for protecting the components of the optical analysis system 10. As shown, sampling of the sample W is accomplished through a window 13 in the enclosed optical analysis system 10. Accordingly, the enclosed optical analysis system 10 can be used in a dangerous (e.g., explosive) environment. As will be described in detail below, the window 13 is transmissive in a known manner in a spectral region of interest.

As briefly introduced above, the illumination sources 14A, 14B are chosen to provide a source light 34, which has a spectral range determined by a spectral range of interest for the intended sample measurement. The illumination sources 14A, 14B are also chosen based on reliability, intensity, temperature generation, and other factors. The illumination sources 14A, 14B are also redundant to further enhance reliability. As shown in FIG. 1, the redundant illumination sources 14A, 14B can be oriented at 90 degrees from each other with a “50-50” beam splitter 36 located near their center point to provide a constant source of illumination.

FIG. 1 further shows a plurality of lenses 16A, 16B, respectively associated with each of the illumination sources 14A, 14B. The lenses 16A, 16B are used to collect the light signal 34 from the illumination sources 14A, 14B and to focus the light signal 34 on a modulator or chopper wheel 18, described below. As shown, the lenses 16A, 16B are positioned to capture as much of the light signal 34 as possible from the illumination sources 14A, 14B. Additionally, a chopper-focusing lens 17 is used to focus as much of the light signal 34 as possible through the chopper wheel 18. The skilled artisan will instantly recognize the lenses 16A, 16B, 17 are selected for focal length, position, material of construction and the like to enhance transmission (reduce loss) of the light signal 34. For example, in the design of the optical path, if the illumination sources 14A, 14B is a lamp, slight magnification or demagnification of the source is generally obtained at the sample W, depending on the ratios of the focal length, e.g., of the lens 16A to that placed after the illumination source 14A to collimate it. Ultimately, the image of the illumination source 14A on the sample W is directed toward the detectors 30, 32 as described below and again with some slight magnification or demagnification, depending on the ratios of the focal length, e.g., of the lenses 16A to that of, e.g., a lens 50 placed before the detector 30 to focus a reflected light 46 onto the detector 30. Thus, it should be understood that there is a relationship between the focal lengths of the lenses 16A, 16B that must be maintained in order to make sure the ultimate image of the source-excited region of the sample W that is formed on the detectors 30,32 is suited to the physical dimensions of the detectors 30,32.

The skilled artisan will further appreciate that the lenses 16A, 16B shown for example in FIG. 1 are plastic, Fresnel lenses well suited for use in an infrared (IR) region of about 1000 nanometers (nm) to about 3000 nm. However, the skilled artisan will understand that the lenses 16A, 16B are not limited to only plastic, Fresnel lenses and that other types of lenses and materials such as glass can be used for these lenses.

As further shown in FIG. 1, the chopper wheel 18 includes a plurality of alternating windows 38 and a plurality of alternating spokes 40. The alternating windows 38 and spokes 40 modulate the light signal 34 from about 50 Hertz (Hz) to about 5000 Hz to enable a plurality of photodetectors 52, 56 in the optical system 10 to perform properly, as will be further described below. As shown in this example, the chopper wheel 18 is a 10-window chopper wheel rotating at 40 Hz, which provides a chopped signal of 400 Hz. The number and arrangement of the windows 38 and spokes 40 and thus, the chopper frequency, are chosen based on several variables, including a rate of motion of the sample material W moving past the sampling window 13; a performance characteristic of the photodetectors 52,56 and amplification system; a predetermined sampling rate of the data collection and analysis system 10; physical properties of a chopper motor (not shown), control system (not shown), and the chopper wheel 18 (including material(s) of the windows 38).

More particularly, the number of windows 38 in the chopper wheel 18 can be adjusted to provide a suitable degree of signal modulation. In one aspect of the disclosure, the chopper wheel 18 has open windows 38 and black spokes 40, which block the light signal 34. In another aspect, different materials can be placed in the windows 38 to provide different spectral characteristics for the various windows 38. Moreover, the transmission characteristic of these windows 38 could be used as further spectral elements. The windows 38 can also contain multivariate optical elements (MOE) such as those described below with respect to a MOE 48 of the MOE detector 30.

FIG. 1 also shows a plurality of bandpass filters or spectral elements 20 located in a path of the light signal 34 after the light signal 34 has passed through the chopper wheel 18. As briefly discussed above, the spectral elements 20 are selected based on a desired application; i.e., to analyze a particular sample W. The spectral elements 20 are chosen so that the spectral region of illumination covers the desired range; i.e., related to a particular chemical material of interest. For example, if 1500-2000 nanometers (nm) of light wavelengths is the desired spectral region, the spectral elements 20 are selected to filter out wavelengths are not in that region. An example of these spectral elements is a SCHOTT brand filter, which can be a long pass, short pass, or band pass filter. By way of further example but not of limitation, some suitable materials for use as the spectral elements 20 are listed in the following table.

TABLE 1 Properties of Select Transmitting Materials SWL LWL Solubility Hardness MP pH Material Comments cm − 1 cm − 1 RI g/100 g Kg/mm 2 ° C. Range AMTIR SeAsGe 11000 593 2.5 0 170 370 1-9 glass BaF 2 Barium 66600 691 1.45 0.17 82 1280 5-8 Fluoride Ca F 2 Calcium 79500 896 1.4 0.0017 158 1360 5-8 Fluoride CsI Cesium 42000 172 1.73 44 20 621 NA Iodide, very hygroscopic Diamond Type IIa, 30000 <2 2.4 0 5700 550  1-14 strong IR fp absorbance between 2700-1800 cm − 1 Ge Germanium, 5500 432 4 0 780 936  1-14 becomes opaque at elevated temperatures KBr Potassium 48800 345 1.52 53 6 730 NA Bromide KCl Potassium 55600 385 1.45 35 7 776 NA Chloride Thallium KRS-5 Bromide/ 17900 204 2.37 0.05 40 414 5-8 Thallium Iodide NaCl Sodium 52600 457 1.49 36 18 801 NA Chloride Polyethylene For Far-IR, 625 <4 1.52 0 110 1.5-14  swells with some organic solvents SiO 2 Silicon 50000 2315 1.53 0 460 1713  1-14 Dioxide Si Silicon, 8900 624.30 3.41 0 1150 1420  1-12 strong IR absorbance between 624-590 cm − 1 ZnS Zinc Sulfide 17000 690 2.2 0 240 1830 5-9 ZnSe Zinc 15000 461 2.4 0 120 1526 5-9 Selenide Note: To convert from wavenumber (cm − 1) to wavelength (μm), divide 10,000 by the wavenumber; e.g., 5500 cm − 1 is equivalent to 1.8 μm or 1800 nm. SWL—Shortest wavelength for transmission, 1 mm, 50% transmission LWL—Longest wavelength for transmission, 1 mm, 50% transmission RI—Refractive Index, at relevant wavelength MP—Melting point

With reference now to FIGS. 1 and 2, the light signal 34 exits the spectral elements 20 and reflects off a first mirror or turning mirror 24. It will be appreciated that although the turning mirror 24 is shown at an angle of about 45 degrees with the light signal 34 reflecting at this angle, the turning mirror 24 can be turned to any desired angle. As known to those skilled in the art, the turning mirror 24 can be a powered turning mirror powered by a battery, by electricity or the like. Further description of power sources and implementation with the turning mirror 24 is not necessary for one skilled in the art to understand this aspect of the disclosure. The skilled artisan will further appreciate that although the turning mirror 24 is shown as a unitary mirror, the disclosure can utilize multiple mirrors arranged in or adjustable to a variety of positions.

As further shown in FIGS. 1 and 2, the filtered and reflected light signal 34 becomes a reflected light 44 after being reflected by the turning mirror 24. The reflected light 44 thus continues down the concentric sampling tube 22, briefly introduced above, in a direction of the sample W. As shown and further described below, the concentric tube 22 includes an inner annular region (also referred to as tube or chamber) 42A and an outer annular region 42B (also, tube or chamber). In this example, the reflected light 44 is reflected along the inner annular region 42A. It will be understood that the illumination sources 14A, 14B and the detectors 30, 32 are shown in an exemplary orientation and can be reversed. It will be further appreciated that the light signal 34 and the reflected light 44 are shown collimated for simplicity. However, the light signal 34 and the reflected light 44 may not be completely collimated because the illumination sources 14A, 14B can be extended rather than point sources.

The focusing lens 26 in FIGS. 1 and 2 is located near an end of the tube 22 proximate the sample W. As shown in this example, the end of the tube 22 is sealed with the transmissive window 13. The transmissive window 13 should be uniformly transmissive across wavelengths, but if it is not, the transmission characteristics of the transmissive window 13 are taken into account for the design of the system 10 and in particular the MOE 48. This embodiment may include an additional focusing lens 66, which can be solid or have one or more apertures as shown in FIG. 1. The additional focusing lens 66 is used to focus or collimate a carrier light 46, described below, in a direction of the tube 22.

As further shown in FIGS. 1 and 2, the focusing lens 26 focuses the reflected light 44 onto, into or near the sample W via the transmissive window 13. In this example, the reflected light 44 is focused with a focal point 0-5 mm into the sample W. In addition to isolating components of the optical analysis system 10 from an external environment, the transmissive window 13 further enables a mixing vessel or container C, which is being tested/sampled into, to remain intact. As shown in this example, a one-inch (inner diameter) Swagelok® brand connector 62, available from Swagelok Corporation, Solon, Ohio, is used to connect the optical analysis system 10 to the mixing vessel C. This arrangement permits the reflected light 44 to be sent down the tube 22 (inner region 42A), interact with the material of interest W, reflect back up the tube 22 (outer region 42B), and be directed to the detectors 30, 32 as further described below.

As most clearly shown in FIG. 2, a tube 58 defines an aperture 60 for passage of the light signal 34 in a direction of the turning mirror 24. Separation of the illumination and reflection light paths or signals 44, 46 can be further defined or separated by physically separating the inner and outer regions 42A, 42B employing the tube 58. Any minimal reduction in light return of the carrier light 46 described below (caused by physical occupation of a portion of the outer region 42B by the tube 58) is offset by improvement in the amount of backscattered radiation returned to the detectors 30, 32 without encountering the sample W.

More specifically, the tube 58 is used to reduce a non-zero background measurement. The non-zero background measurement can occur in an optical system when a small amount of scattered light is returned to a detector even when no sample is present. Some of the scattered light can be reflected from a window, and some can come from the lenses themselves.

FIG. 2 shows that the tube 58 placed around the mirror 24 before the lens 26. The tube 58 reduces background signals by separating the excitation and collection light paths 34, 46 to minimize “cross-talk”. As shown, the tube 58 defines an aperture 60 for passage of the light signal 34 in a direction of the turning mirror 24. As further shown, a conical extension 58A of the tube 58 can be placed after the mirror 24 in a direction of the detector 30. A thickness of the tube 58 is minimized.

Also shown in FIG. 2, the tube 58 can have specular interior and exterior surfaces as well as a highly reflective coating 58B, such as gold, applied by electrolysis deposition, evaporation or other thin film coating method. The coating 58B reflects rays 34, 46 that would ordinarily terminate at a surface of the tube 58 back into respective optical paths from which they came. Although an image of the illumination source 14A, 14B may be vignetted, the “lost” light in the image is still focused to a spot within the zone illuminated by the illumination source 14A, 14B. Likewise, the returning light outside the tube 58 can be kept from being lost by traveling inside an outer tube with a specular reflecting surface (not shown, but surrounding the outer light path). This will keep light loss to a minimum while keeping the input and output paths relatively isolated from one another.

As introduced above, the reflected light 46 shown in FIGS. 1 and 2 travels back down the outer annular region 42A of the sampling tube 22, past the turning mirror 24. The light 46 reaches the beam splitter 28 (one of its operating positions shown in phantom). The beam splitter 28 divides the light 46 with a neutral or gray spectrum, sending some of the light 46 in a direction of the first or Multivariate Optical Element (MOE) detector 30 through the MOE 48, briefly introduced above, and through a first lens 50 onto the photo detector 52, also briefly introduced above. The beam splitter 28 sends some other portion of the light 46 through a second lens 54 onto the other detector 56, also briefly introduced above.

As shown in the following table by way of example, but not of limitation, some detectors suitable for use as the detectors 52,56 include:

TABLE 2 Cut Off Operating Wave Detectivity Frequency Temperature Detector Types¹ Range (λμ) D² (H_(z)) (K) Pt—S PV 0.35-0.6  30 10⁸ 295.0 Si p-n PD PV 0.4-1.0 50 10⁷ 295.0 Si p-i-n PD PV 0.4-1.1 80 10⁸ 295.0 Si APD PV 0.4-0.8 80 10¹⁰ 295.0 Ge p-n PD PV 0.6-1.8 50 10⁷ 295.0 InSb p-n PD PV 3.0-6.2 8 5 × 10² 77.0 PbSnTe p-n PV  5.0-11.4 >15-60 V/W  10 77.0 PD PbS PC 0.5-3.8 15.00 300 196.0 PbSe PC 0.8-4.6 3.00 3 × 10³ 196.0 PbTe PC 0.8-5.5 0.16 3 × 10³ 196.0 p-InSb PC 2.0-6.7 2.00 2 × 10⁵ 77.0 n-InSb PC 1.0-3.6 30.00 2 × 10⁶ 195.0 PbSnTe PC  5.0-11.0 1.7 8 × 10⁵ 4.2 CdHgTe PC  5.0-16.0 3.00 10⁴ 4.2 Ge: Au PC 2.0-9.5 0.02 10⁴ 77.0 Ge: Zn, Au PC  5.0-40.0 1.00 10³ 4.2 Ge: Cu PC  5.0-30.0 3.00 10³ 4.2 Si: A1 PC  2.0-16.0 1.00 10⁴ 27.0 Si: Sb PC  2.0-31.5 1.80 10⁴ 4.0 ATGS TC   1-1000 0.030  10 295.0 (Ba,Sr)TiO₃ TC   1-1000 0.011 400 295.0 Si — 0.2-1.1 — — — Ge — 0.4-1.8 — — — InAs — 1.0-3.8 — — — InGaAs — 0.8-3.0 — — — InSb — 1.0-7.0 — — — InSb (77K) — 1.0-5.6 — — — HgCdTe (77K) —  1.0-25.0 — — — Note 1: PV-photo transistor type; PC: photo conductive detector type; TC: pyroelectric detector type Note 2: (10¹⁰ cmHz^(1/2) W¹)

As further shown in FIG. 1, a gain mechanism 64 is in communication with the detectors 30, 32 and the MOE 48. The gain mechanism 64 weights a magnitude of the property of an orthogonal component of a portion of the carrier light 48 as described, for instance, by Myrick et al. in U.S. Pat. No. 6,198,531 B1 and in U.S. Pat. No. 6,529,276 B1 to Myrick.

As briefly introduced above, the beam splitter 28 is not required in an alternative embodiment of the disclosure in which a signal from the sample W is analyzed using a PCR-type model in an off-line approach. This alternative embodiment and approach is useful, for instance, for studying signals independently. More particularly, a system substantially as described above but without the beam splitter 28 is used to take an integral of the light on a detector similar to the detector 30 described above. By analyzing frequency-dependent intensities, results similar to those of the foregoing embodiment are produced, although possibly with a relatively slower response time in the present embodiment.

Also, in an additional aspect of the disclosure as shown in FIG. 1, a system 68 using an electrochemical or chemometric model can be employed in conjunction with any of the foregoing embodiments to make similar or same measurements of the light 46 reflected from the sample W as the measurements described in the foregoing embodiments. By way of example but not of limitation, the system 68 may be one as described by Myrick et al. in PCT Application Number PCT/US2004/043742, based on U.S. Provisional Application No. 60/533,570, filed Dec. 31, 2003, which are incorporated herein by reference thereto.

In addition to the reflectance mode described above, one or more optical analysis systems can operate in a transmission mode in conjunction with the foregoing embodiments. In such a case, light is directed (passes) through the sample W, e.g., a fluid sample, and collected on another side of the sample W to enable study of particle density in the fluid in conjunction with the chemical content described above. For instance, the system 10 can be configured to operate in transmission mode where the light is shone through the sample W to a similar detection system 110 as shown in FIG. 1 in phantom for clarity). Additionally, or alternatively, a mirrored surface 210 can be placed within the transmissive sample W to reflect the light back into the system 10.

With reference now to FIG. 3, a second exemplary embodiment of the present subject matter is designated generally by reference number 110. Many aspects of the optical analysis system 110 and related components are similar to the foregoing embodiment; thus, for the sake of brevity, only certain differences are described below. However, to provide a full and enabling disclosure of the optical analysis system 110, when like or similar elements and components are not specifically described below; implicit reference is made to the foregoing descriptions.

As shown in FIG. 3, the optical analysis system 110 broadly includes a housing 112, an illumination or light source 114, a chopper wheel 118, one or more spectral elements 120, a beam splitter 128, a first detector 130 including a multivariate optical element 148, and a second detector 132. The optical analysis system 110 further includes an electrical connection 160, a pressurization sensor 162 and a purge gas assembly 164, which those skilled in the art will readily understand; therefore, further description is not necessary to understand and practice these aspects of the disclosure.

With more particular reference to FIG. 3, the illumination source 114 provides a light 134, which passes through a collecting Fresnel lens 116A and into and through the spectral element(s) 120. In this example, the illumination source 114 is rated for at least about 10,000 hours of operation, which alleviates a need for redundant illumination sources though they may be provided if desired. Also in this example, the collecting Fresnel lens 116A is sized to be about 1.5 square inches and is spaced about 0.6 inches from the illumination source 114. The skilled artisan will instantly recognize that these dimensions can be adjusted according to particular system requirements and are not meant as limitations of the disclosure.

As further shown in FIG. 3, the light 134 passes through the spectral elements 120, which filter out undesired wavelengths to define a desired spectral region, e.g., 1500-2000 nm, in order to target a particular chemical material of interest. The light 134 is focused by focusing Fresnel lens 116B, which is also sized to be about 1.5 square inches and spaced about 1 inch from the chopper wheel 118. As shown, the chopper wheel 118 reflects a portion of light 134 as a calibration or reference light 135 and a transmitted light 144. Calibration light 135 is collimated by lens 158 before reflecting from a first mirror 124A through an adjustable aperture 112B in a bulkhead 112A of the housing 112. The aperture 112B is adjustable to dictate a desired amount of the calibration light 135. Finally, calibration light 135 impinges on beam splitter 128 thereby sending a portion 135A of calibration light 135 to the first MOE detector 130 and a portion 135B of calibration light 135 to the second or baseline detector 132.

FIG. 3 further illustrates that transmitted light 144 passes from the chopper wheel 118 into a collimating Fresnel lens 136, which in this example is sized to be about 1.5 square inches and is spaced about 0.6 inches from the chopper wheel 118. The transmitted light 144 passes through another adjustable aperture 112C in the bulkhead 112A and impinges upon a second mirror 124B, which directs the transmitted light 144 toward a sample M in a container C, such as mixing vat or blender. The skilled artisan will recognize that the container could be a conveyor belt or other device for holding or transporting the sample M and is not limited to an enclosed container.

As shown in FIG. 3, the transmitted light 144 passes through a transmissive window 113 and enters the container C and on through the sample M. The sample M may be a substantially transparent liquid, such as water, petrochemicals, or the like but can also be any relatively clear product such as gelatin capsules containing a pharmaceutical product. As shown, a focusing lens 126, which in this example may be round in shape, may be positioned adjacent to or as much as one inch from an outer surface of the container C. The transmitted light 144 passes through the sample M and reflects from the focusing lens 126 as a carrier light 146. Further details of the focusing lens 126 are described below with respect to a similar lens 226 as shown in FIGS. 4A, 4B and 5.

Continuing with reference to FIG. 3, the carrier light 146 may be directed by the tube 122 in a direction of the first detector 130. Eventually, the carrier light 146 impinges on the beam splitter 128 and a portion passes in a direction of the detector 132 for baselining with the portion 135B of the calibration light 135. Another portion of the carrier light 146 passes through MOE 148, which as noted above, has been selected for the chemical of interest based on the various components of the system 110. Finally, that portion of the carrier light 146—having passed through the MOE 148—is focused by lens 150 and received by the detector 152. As described above, the two signals collected by the detectors 132, 152 can be manipulated, e.g., mathematically, to extract and ascertain information about the sample carried by the carrier light 146.

Turning now to FIGS. 4A and 4B, detailed views of a retroreflector or collimating mirror 226 are shown. In this example, the mirror 226 is similar to the mirror 126 introduced above and is generally cylindrically shaped with a first end 226A and a second end 226B. The mirror 226 is also coated with a reflective surface such as aluminum (Al), gold (Au) or other elements or and materials or combinations thereof as dictated by the desired spectral region. The skilled artisan will appreciate that other shapes and reflective coatings can be provided to meet specific design requirements and characteristics of the target sample; thus, the mirror 226 is not limited to the exemplary embodiment shown in FIGS. 4A and 4B.

With reference to FIGS. 3, 4A and 4B, the mirrors 126, 226 are useful for analyzing translucent liquid samples, for example, since liquids, in contrast to powders, do not readily create a diffuse reflectance to produce the desired carrier light 146 as shown in FIG. 3. By way of example operation, the lens 126 in FIG. 3 may be removed and replaced with the mirror 226 for retroreflection of the light 144 for transreflection measurement of the carrier light 146 for liquid sample analysis.

Turning now to FIG. 5, as the light 144 passes through the mirror 126, the light 144 is collimated into the liquid sample in the container C as in FIG. 3. As shown in FIGS. 3 and 5, the carrier light 146 reflects from the liquid sample and returns through the first end 126A, which defines one or more conical shaped depressions or indentations 126C. The conical shaped indentations 126C act to diffuse the carrier light 146, and the carrier light 146 is directed through the MOE 148 as described above.

In contrast to the discovery shown in FIG. 5, a conventional flat mirror 901 and a light 903 are arranged in a conventional manner as shown in FIG. 6. The light 903 shines light rays 905 in a direction of the flat mirror 901, which reflects light rays 907 along the same ray path as the emitted light rays 905. Accordingly, any information carried by the light rays 907 reflecting from the flat mirror 901 would at least interfere with the light 903 and possibly be unreadable by a detector 909 offset from the light 903 due to interference with the light rays 905.

The skilled artisan will appreciate that the disclosure is not limited to the foregoing exemplary arrangements. For example, the system can be arranged with the mirror 126 and the detectors 152, 156 on an opposite side of the container C such that the light 146 passes through the liquid sample into the mirror 126. Accordingly, in this alternatively arranged system, particle density in a fluid can be studied in conjunction with a chemical content of the fluid.

Dynamic Real-Time Detection and Measurement

The functionality of the MOC system 10 or 110 as described above allows for the collection of the entire spectral range of testing simultaneously. This is notably different than either a system based on either a scanning lamp or detector system or a discrete diode array detection system. The ability to monitor over the complete spectral range of interest opens up a re-definition of the term “real-time” measurement and analysis.

For instance, true “real-time” process measurements are possible where “real time” refers to obtaining data without delays attendant to collecting samples or delays due to lengthy computer processing of measurement signals. For example, in exemplary methods described below, process data can be obtained in an instantaneous or near-instantaneous manner through using measurement techniques to directly monitor materials of interest while such materials are undergoing process steps. Long delays due to processing of measurement signals are avoided by optically processing the light as it is reflected from the material(s) of interest.

Although specific examples disclosed herein present monitoring the blending of a powdered material and examining solid tablets, the concept can be extended to other phases as briefly introduced above. Thus, the present systems and methods can be utilized to analyze solids, solutions, emulsions, gases, dispersions and the like. In addition, while exemplary embodiments discussed herein use reflectance measurements, measurements in a transmission or transflectance mode would also be appropriate.

One of ordinary skill in the art will recognize that differing applications may require modifications and alterations to certain components in order to take full advantage of the presently-disclosed systems. For instance, more diffusion of light has been observed in solid powders relative to liquids; accordingly, different lenses may be needed when a liquid is monitored in order to account for such variations and achieve more accurate measurements.

The presently-disclosed technology can be applied to real-time measurements for a range of industrial applications. These include, but are not limited to monitoring of the blending of pharmaceutical powders, including excipients, additives, and active pharmaceutical materials; blending of other powders, including food and chemicals; monitoring dispersions and bi-phasic mixtures (such as insulin, emulsions); and oil and gas applications, including analyzing water content in oil, or oil content in water.

Inclusion of a transmissive window provides physical separation between the measuring device and the process or material being tested. Therefore, this window allows for in-line measurement and/or non-invasive measurement of parameters such as chemical functionality, including alcohol content of petroleum fractions or tackifier resins. Environmental applications are also conceivable, such as stack gas analysis, including measurement of NOx, SOx, CO, CO2, or other gases in a gas stream; wastewater analysis and treatment monitoring; and hazardous substance monitoring applications such as mercury vapor detection.

Real Time Measurement of Powder Mixing

As noted above, MOC technology can be used to monitor a wide variety of materials as the materials are subjected to different processes. For instance, the mixing of powders can be monitored. As materials are blended, the existing art does not allow for continuous, real-time, in-line measurement. Current limitations are the result of several factors including: moving of the powders being measured during the course of data acquisition and the need to connect analytical equipment to the measurement point using fiber optic cables. This optical analysis system is designed to allow for instantaneous measurement using a measurement point located on the vessel.

To measure the composition of the mixture of powders during blending, the system is located in a position to shine the sampling beam into the mixture. An exemplary implementation of such a measurement technique is illustrated in FIG. 7. An optic head 510 includes a housing 512 and requisite MOEs and spectral elements to obtain desired information about a material of interest. The optic head 510 is generally configured and constructed in accordance with the embodiments discussed above in conjunction with FIGS. 1-5.

In discussing various embodiments below, the term “optic head” is used in place of the term “measurement system” in referring to the light, lenses, spectral elements, and detectors of the optical computing unit discussed above. As will be apparent to one skilled in the art, a complete measurement system may utilize several instances of the optical computing unit, and so the term “optic head” is used as a shorthand reference to a single instance of the optical computing unit.

With more particular reference to FIG. 7, the optic head 510 is connected via an umbilical 514 to an appropriate power supply and analysis computer or computers (such as system 68 described above) also configured in accordance with the principles of MOC analysis. As shown, a process point including a mixing blender bowl 522 containing mixture 524 may thereby be monitored via the optic head 510.

FIG. 7 further shows a port or connection 520 such as a Swagelok® brand pharmaceutical-grade stainless steel port introduced above. The connection 520 connects an opening 518 of the mixing blender bowl 522 to an optic head inlet 516. The inlet 516 includes the window (13 or 113 in the embodiments discussed above) through which light is transmitted and reflected for materials analysis while keeping the material monitored separate from the internal components of the optic head 510.

By way of example, the optic head 510 in FIG. 7 can be configured to monitor the concentration of a mixture of aspirin and lactose. Accordingly, a sapphire window (e.g., window 113 in FIG. 3) may be positioned at the end of the optic inlet 516 for interrogating the powder, and the optic head 510 may be configured with MOEs designed to monitor aspirin concentration. More specifically, a 20-watt Gilway lamp may be modulated using 5mm D2O and 5 mm Germanium spectral elements, and the modulated light may be directed into the powder. The reflected light from the powder is directed through the MOEs onto a PbS detector. A portion of the modulated light, as discussed above, is preferably directed into a second detector. The resulting PbS detector signal can be compared against the second detector signal in order to determine the concentration of aspirin. For example, a concentration graph 526 as shown in FIG. 7 may be obtained, which shows a rise in aspirin concentration as aspirin is added. FIG. 7 further shows a “leveling-off” (asymptote phenomenon) as the mixing process continues.

The skilled artisan will appreciate that other embodiments in which transmitted light is to be measured would utilize two ports, preferably located opposite one another with the measured sample passing between the two ports.

Real Time Measurement of Chemicals/Flowing Materials

Other embodiments of the present disclosure include real time measurement of flowing materials. In such embodiments, the sampling window(s) may be located on a pipe or vessel such that interrogating illumination can be applied to the material. For instance, a port similar to the port 520 in FIG. 7 could be included on a pipe to allow for sampling of the material inside the pipe. A window as described above may be positioned directly on the pipe, or on a small diversion away from the main flow path, as appropriate under certain circumstances. Such embodiments could also include sampling of vapor systems within a stack to monitor combustion gases or flowing process stream such as water containing other materials.

Real Time Measurement of Moving Containers

Still further embodiments of the present disclosure include the real time measurement of materials in containers, such as vials or bins where the container is either at least partially open to the outside environment or transmissive to the sampling illumination. Such containers could be stationary or in motion. A container could also include a conveyor or trough carrying material. Typical applications could include the monitoring the progress of a chemical reaction or the content of samples moving past a measurement location.

For instance, FIG. 8 illustrates a plurality of samples 552′ positioned on a rotating disc conveyor 550′. Although a disc conveyor is shown, one of ordinary skill in the art will recognize that the samples 552′ may be positioned on a conveyor belt or other automated conveyance, depending upon the particular testing circumstances and environment. Also, although the samples 552′ are illustrated as tablets in FIG. 8, the samples 552′ could be or include capsules, caplets, pills, and other individualized units of pharmaceutical product (or other consumable product).

As further shown in FIG. 8, the tablets 552′ are rotated into the view of an optical inlet 516′ of an optic head 510′, which is similar to the discussion above and may include a housing 512′ and an umbilical 514′, as well as requisite internal components, filters, and MOEs to perform the desired testing operations. Likewise, this exemplary system and process may be configured to monitor around 5 tablets per second, with the tablets 552′ being in continuous motion.

As discussed in conjunction with the optic head 510 in FIG. 7, in the embodiment of FIG. 8, a PbS detector can be used in conjunction with a sapphire window and D20 and germanium spectral elements to monitor the concentration of aspirin and lactose. In contrast to the system of FIG. 7, the sapphire window of the optic inlet 516′ is positioned above the samples 552′ such that a beam of light 544′ is focused downward onto the samples 552′ on the conveyor 550′. However, the optical principles described above remain the same. As shown, a graph 528′ represents exemplary results that would be obtained from the samples 552′ of varying concentration of aspirin, with each spike representing an individual one of the samples 552 being in full view of the optic head 510′.

The samples 552′ may be actual samples to be measured, such as the tablet end-product illustrated in FIG. 8 and discussed below in conjunction with FIG. 9. However, one of ordinary skill in the art will recognize that the samples 552′ may also include transparent containers and the like, which may contain a dispersion or suspension of a solid material in a liquid or a solution, or solid materials. For instance, trays of powder can be placed on an automated conveyance and brought into view of optic head 510′ in a manner similar to the method described in FIG. 8.

Additionally, instead of moving the samples 552′, one of ordinary skill in the art will note that measurement device 510′ could be repositioned to examine the samples 552′ by appropriate machinery such as overhead tracks, robotic arms, and the like. The skilled artisan will recognize that in such cases, appropriate care would preferably be taken to ensure that force levels applied to the measurement device and its internal components remained within tolerable levels.

Integrated Real-Time Process Management Using MOC Systems

Turning now to FIG. 9, an embodiment of real-time process management is schematically depicted. As shown, a plurality of optic heads 710 are integrated into various process steps 720, 730, and 740. The process steps 720, 730, and 740 can represent stages or steps of any number of industrial operations in which materials are handled or manipulated, and in which physical state or compositional data is desirable. In accordance with the system embodiments discussed above, each optic head 710 a, b, c, d, e is provided with MOEs and other optical components specifically tailored to the materials characteristics, which are to be monitored at each step, and interfaced with process control computer(s). The analysis data ultimately provided by collection points 710 is shown at 722, 724, 732, 742, and 744. Such data can be obtained using single or multiple process control computers configured to collect, analyze, and otherwise handle the data from the detectors within the optic heads in accordance with the principles of multivariate optical computing discussed above.

Assume, for example, that process steps 720, 730, and 740 represent various stages in a pharmaceutical manufacturer's production line for blending powder and forming tablets. The skilled artisan will recognize that pharmaceutical manufacturing often entails strict control and monitoring of material composition and mixing at every stage of production.

The initial steps of obtaining and readying component materials in a pharmaceutical process could be represented at 720 in FIG. 9. The optic head 710 a could be used to monitor the incoming raw materials in trays or on conveyors and provide inspection and quantification data 712, such as purity data. Optic head 710 b could be configured to the monitor incoming material(s) as they undergo an initial process stage, for example, providing chemical drying characteristics 724 as the raw materials are dried.

The process step 730 in FIG. 9 could represent mixing of active and excipient components into a powder, and optic head 710 c could provide data 732 on mixing progress. For instance, the optic head 710 c could be interfaced with the mixing container and provide data tracking active ingredient concentration over time as in FIG. 7. Based on such concentration, requisite steps could be taken to ensure the optimal amount of active component is in the resulting mix or otherwise adjust the mixing process by altering temperature or the like.

As further shown in FIG. 9, step 740 could represent pressing tablets, with optic heads 710 d and 710 e positioned above a conveyor moving the completed tablets, and providing data 742 on tablet components and homogeneity, as well as data on coating thickness and uniformity 744.

FIG. 9 further shows a step 750 representing the final portions of the manufacturing process, which are not monitored, such as packaging. One skilled in the art will recognize, however, that step 750 could represent the entry into a different process, which is itself monitored by one or more optical analysis systems as described herein.

Attention is now directed to the exemplary embodiments of the present disclosure as illustrated in FIGS. 10 and 11. The skilled artisan will note that prior exemplary embodiments discussed reflective measurements, while noting such embodiments could be suitably configured for use in transmissive measurement schemes. FIGS. 10 and 11 illustrate examples of such configurations.

In FIG. 10, for instance, a multivariate optical measurement system 310 is configured in a manner similar to the embodiment discussed with respect to FIG. 3, above. However, a light diversion path 370 in one embodiment includes a fiber-optic cable having ends 372 and 374 has been included to divert light 344 emanating from a source 314 into the tested material M such that the light 344 is transmitted through material M and into the remaining elements (i.e. detectors, MOEs). The light diversion path is not limited to a fiber optic cable and could be mirrors in series (as shown in phantom for clarity).

As shown in FIG. 10, the light 344 enters end 372 of diversion path 370 after passing through Fresnel lenses and spectral elements 320 and modulating chopper wheel 318. However, one skilled in the art will recognize that the point of diversion may be varied according to the particulars desired in a system. For instance, the beginning 372 of path 370 could be placed on the other side of optional aperture 312C. Also, although a collimating lens such as the collimating lens 136 of FIG. 3 is not shown in FIG. 10, such a lens, or other suitable optical components, could be placed at end 372 of path 370 to appropriately condition light 344 for optimal measurement via transmission through material M. Similarly, optical components, such as a focusing lens or a spectral element, could be included at diversionary path outlet 374; such placement is illustrated by element 574 shown in phantom in FIG. 11 and further described below. Moreover, the path 370 in FIG. 10 could include other means and methods for directing the path of light, such as the above-described fiber optic cable, mirrors, or a variant of the tube and mirror combination discussed in conjunction with other embodiments of the present disclosure, for example.

As further shown in FIG. 10, a light 346 transmitted through material of interest M passes through window 313 and lens 326 and into the remaining components of the multivariate optical system in a manner similar to the foregoing descriptions. Depending upon the particular implementation of a measurement system, window 313 and/or lens 326 may be varied or removed depending upon the light intensity and focus that is needed to optimize measurements by detectors 352 and 356.

Turning now to FIG. 11, an implementation of transmissive measurement using diverted illuminating light is shown. As discussed previously in conjunction with FIGS. 7 and 8, portions of a measurement system may be adapted for housing within an optic head as described above. Thus, an optic head 510″ may be internally configured with lamps, spectral elements, MOEs and the like in accordance with the principles of multivariate optical computing and measurement. As shown in this example, optic head 510″ includes housing 512″ and inlet point 516″.

The optic head 510″ in FIG. 11 is further adapted to house an optical measurement system such as the one discussed above in conjunction with FIG. 10 to route illuminating light into a material opposite the inlet point 516″ to allow for transmissive measurements using optic head 510″. As shown, an exemplary diversion path 570″ runs from optic head 510″ to an output point 574″. Light is transmitted through sample 552″ (corresponding to material M of FIG. 10) and into inlet point 516″ of the optic head 510″ for optical processing and detection. One skilled in the art will recognize that the conveyor disc 550″ would be configured such that light emitted from 574″ is not blocked.

As noted previously, ghosted portion 574″ indicates optional light conditioning and/or other interface components which may be appropriate for a particular implementation. For example, depending upon the sample 552″ analyzed, different focal points may be selected using a focusing lens positioned at 574″. If the sample 552″ comprises a pill, the light can be focused at the center of the pill for determining composition, or at the periphery of the pill to analyze the content of a coating. Lenses of different focal lengths could be selected depending upon the particular geometry and measurement needs.

Although a plurality of discrete samples resting on a conveyor are illustrated in FIG. 11, the principles illustrated are applicable to other phases and configurations of materials. For example, ghosted container C of FIG. 10 could be substituted for the conveyor 550′ of FIG. 10 for measurement of material M disposed in a mixer, pipe, or other vessel in a manner similar to that shown in FIG. 7. In such configurations, optic head inlet point 516″ (including window 13,313) would be proximate to the pipe or mixer wall, and could be interfaced using a port or connector such as the port 520 discussed in conjunction with FIG. 7. In such embodiments, endpoint 574″ could comprise a additional port and window to directly interface the end of path 570″ with the container C so that light exiting path 570″ would travel through the material in the container and then into inlet point 516″. In that manner, real-time transmissive measurement of continuous processes is conceivable.

The disclosure may be better understood from the following tests and examples.

EXAMPLE I/SYSTEM I

A first breadboard system was constructed and used to test a mixture of powders.

System I Components:

-   Illumination: 20 W Gilway lamp -   Spectral Elements: 5 mm deuterium oxide (D₂O), 5 mm Germanium -   Optical Window: fiber optic probe -   Detector: InAr detector from Judson -   MOE: specific to test

Procedure and Results of Static Testing Using System I:

A powdered sample with a known composition was placed in a dish and the fiber optic probe was placed in contact with the powder. The output of the detectors was monitored and recorded.

EXAMPLE II/SYSTEM II

A system similar to the optical analysis system 10 shown in the figures was constructed and used to make static measurements on aspirin/lactose.

System II Components:

-   Illumination: 20 W Gilway lamp -   Spectral Elements: 5 mm D2O, 5 mm Germanium -   Optical Window: none -   Detector: PbS detector from New England Photoconductor -   MOE: specific to test conditions.

Procedure and Results of Static Testing Using System II:

A powdered sample with a known composition was placed in a dish and the system light beam was focused on the powder. The output of the detectors was monitored and recorded. Aspirin/lactose samples covering the range of 100% aspirin to 100% lactose were tested.

EXAMPLE III/SYSTEM III

A system similar to the optical analysis system 10 shown in the figures was constructed and used to make dynamic measurements on aspirin/lactose.

System III Components:

-   Illumination: 20 W Gilway lamp -   Spectral Elements: 5 mm D2O, 5 mm Germanium -   Optical Window: sapphire window -   Detector: PbS detector from New England Photoconductor -   MOE: specific to test conditions.

Procedure and Results of Dynamic Testing Using System III:

The aspirin/lactose testing was made on a mixer bowl containing lactose and the system measured as aspirin was added to the system and mixed. Specifically, lactose powder was placed in the bowl of a mixer and the measurement system was attached the bowl using a Swagelok® brand fitting. A sapphire window was used to contain the powder in the bowl and allow the system to interrogate the powder. With the mixer turning, known amounts of aspirin were added and the system output signal was monitored and recorded. Aspirin was added in several allotments to about 37% final aspirin concentration.

EXAMPLE IV/SYSTEM IV

A system similar to the optical analysis system 10 shown in the figures was constructed and used to make static measurements on aspirin/lactose.

System IV Components:

-   Illumination: 5 W Gilway lamp -   Spectral Elements: 5 mm D2O, 5 mm Germanium -   Optical Window: none -   Detector: PbS detector from New England Photoconductor -   MOE: specific to test conditions.

Procedure and Results of Dynamic Testing Using System IV:

Similar to the examples above.

EXAMPLE V/SYSTEM V

A system similar to the optical analysis system shown FIG. 3 was constructed and used to make dynamic measurements of water/hydraulic fluid mixtures.

System V Components

-   Illumination: 20 W Gilway lamp -   Spectral Elements: 5 mm Germanium -   Optical Window: sapphire window -   Detector: PbS detector from New England Photoconductor -   MOE: specific to test conditions.

Procedure and Results of Testing Using System V:

Samples of automobile brake fluid were prepared with various levels of water; e.g., between 0% and 3% water. The liquid samples in quartz cuvettes with a 2 mm path length were analyzed using the system. The cuvettes were placed horizontally on a moving platter; the system was located above the platter; and the conical mirror was located below the platter.

Although various aspects of the disclosure have been described in such a way as to provide an enabling disclosure for one skilled in the art to make and use the systems and methods according to the disclosure, it should be understood that the descriptive examples of the disclosure are not intended to limit the present disclosure to use only as shown in the figures. For instance, the housings can be square or oval shaped, or a variety of other shapes. Further, a variety of light sources can be substituted for those described above. It is intended to claim all such changes and modifications as fall within the scope of the appended claims and their equivalents. Thus, while exemplary embodiments of the disclosure have been shown and described, those skilled in the art will recognize that changes and modifications may be made to the foregoing examples without departing from the scope and spirit of the disclosure. 

1. An optical analysis system, comprising: a light source being configured to radiate a first light along a first ray path; a modulator disposed in the first ray path, the modulator being configured to modulate the first light to a desired frequency; a spectral element disposed proximate the modulator, the spectral element being configured to filter the first light for a spectral range of interest of a sample, the first light being directed into the sample; a retroreflector being configured to convert the first light from the sample into a second light; a beamsplitter being configured to split the second light into a first beam and a second beam; an optical filter mechanism disposed to receive the first beam, the optical filter mechanism being configured to optically filter data carried by the first beam into at least one orthogonal component of the first beam; a first detector mechanism in communication with the optical filter mechanism to measure a property of the orthogonal component to measure the data; and a second detector mechanism being configured to receive the second beam for comparison of the property of the orthogonal component to the second beam.
 2. The optical analysis system as in claim 1, wherein the retroreflector includes a coating of gold or aluminum.
 3. The optical analysis system as in claim 1, wherein the retroreflector is a collimating mirror being configured to diffuse the first light into the second light.
 4. The optical analysis system as in claim 1, wherein the retroreflector is a conical mirror.
 5. The optical analysis system as in claim 1, wherein the sample is substantially transparent.
 6. The optical analysis system as in claim 1, wherein the sample is a liquid.
 7. The optical analysis system as in claim 1, further comprising a cavity in communication with the spectral element, the cavity being configured to direct the first light in a direction of the sample.
 8. The optical analysis system as in claim 7, wherein the cavity is further configured to direct the second light.
 9. An optical analysis system, comprising: a light source being configured to radiate a first light along a first ray path; a modulator disposed in the first ray path, the modulator being configured to modulate the first light to a desired frequency; a spectral element disposed proximate the modulator, the spectral element being configured to filter the first light for a spectral range of interest of a sample; a light diversion path for diverting the first light into the sample, the first light being transmitted through the sample and emerging as a second light; a beamsplitter being configured to split the second light into a first beam and a second beam; an optical filter mechanism disposed to receive the first beam, the optical filter mechanism being configured to optically filter data carried by the first beam into at least one orthogonal component of the first beam; a first detector mechanism in communication with the optical filter mechanism to measure a property of the orthogonal component to measure the data; and a second detector mechanism being configured to receive the second beam for comparison of the property of the orthogonal component to the second beam.
 10. The optical analysis system as in claim 9, wherein the light diversion path includes a fiber-optic cable or a plurality of mirrors.
 11. A method of high-speed processing and monitoring, comprising: moving a product past an inspection point; illuminating at least a section of the product with a light; directing the light that has passed through the section and is carrying information about the product through at least one multivariate optical element to produce a first signal; deflecting a portion of the light to produce a second signal; detecting the first signal at a first detector; detecting the second signal at a second detector; and determining at least one property of the product based upon the detector outputs as the product moves past the inspection point at a rate of about one section per second to about five sections per second.
 12. The method as in claim 11, wherein the product is one of a solid product, a liquid product or a gas product.
 13. The method as in claim 12, wherein the solid product is a pharmaceutical tablet or a pharmaceutical powder.
 14. The method as in claim 11, wherein the product is an emulsion.
 15. The method as in claim 11, wherein the product is a solution.
 16. The method as in claim 11, wherein the product is a mixture.
 17. The method as in claim 11, wherein an illumination source for the light is disposed proximate the section of the product and the light that has passed through the section is reflected from the section in a direction of the detectors.
 18. The method as in claim 11, wherein an illumination source for the light is disposed proximate the product and the light that has passed through the section transmits through the product in a direction of the detectors.
 19. The method as in claim 18, further comprising diverting a part of the light from the illumination source into the product along a light diversion path.
 20. The method as in claim 19, wherein the light diversion path includes a fiber-optic cable.
 21. The method as in claim 18, further comprising diffusing the light that has passed through the section before the light is directed to the multivariate optical element.
 22. The method as in claim 19, wherein the light is diffused by a collimating mirror.
 23. A method of processing and monitoring a product, the method comprising: introducing a product at an inspection point; illuminating the product with a spectral-specific light though an optic lens; directing the light that has passed through at least a section of the product through at least one multivariate optical element to produce a first signal, the directed light carrying information about the product; detecting the first signal at a first detector; deflecting a portion of the directed light to produce a second signal in a direction of a second detector, the second detector configured to detect the second signal; and determining at least one property of the product at a rate of about one section of the product per second to about five sections of the product per second based upon the detector outputs.
 24. The method as in claim 23, wherein the product is a pharmaceutical tablet or a quantity of pharmaceutical powder.
 25. The method as in claim 23, wherein the product is one of a solid product, a liquid product or a gas product.
 26. The method as in claim 23, wherein the product is disposed in a closed container, the container at least partially transparent to light focused onto the product.
 27. The method as in claim 23, further comprising moving the product past the inspection point.
 28. The method as in claim 23, further comprising moving the optic lens past the product. 